Canonical Allele Identifier: CA9129755
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs764703923
gnomAD v2: 19-6714295-C-T
gnomAD v3: 19-6714284-C-T
gnomAD v4: 19-6714284-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714284C>T , CM000681.2:g.6714284C>T GRCh38
NC_000019.9:g.6714295C>T , CM000681.1:g.6714295C>T GRCh37
NC_000019.8:g.6665295C>T NCBI36
NG_009557.1:g.11368G>A , LRG_27:g.11368G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.477-36G>A ENSP00000512083.1:n.477-36G>A
ENST00000245907.11:c.600-36G>A MANE Select ENSP00000245907.4:n.600-36G>A
ENST00000245907.10:c.600-36G>A ENSP00000245907.4:n.600-36G>A
ENST00000595577.1:n.68G>A
NM_000064.3:c.600-36G>A NP_000055.2:n.600-36G>A
NM_000064.4:c.600-36G>A MANE Select NP_000055.2:n.600-36G>A